| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.040 | 16 | 67868167 | intron variant | G/A | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 1 | 222653139 | intron variant | G/A;C | snv | 0.64; 1.2E-05 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.040 | 3 | 138401110 | intron variant | T/C | snv | 0.12 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 109457363 | non coding transcript exon variant | C/G | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.882 | 0.120 | 9 | 22132077 | downstream gene variant | A/G;T | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 114914926 | regulatory region variant | G/A | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 1 | 56543106 | intron variant | C/T | snv | 7.6E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.882 | 0.080 | 10 | 30046193 | intron variant | T/C | snv | 0.33 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 9 | 104832083 | intron variant | A/G | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 16 | 67979568 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.040 | 16 | 67991092 | intron variant | G/A | snv | 0.17 | 0.17 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.851 | 0.200 | 12 | 120951159 | intron variant | A/C | snv | 0.70 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.882 | 0.080 | 12 | 89615182 | intron variant | A/G | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.040 | 1 | 239273242 | intergenic variant | A/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.080 | 14 | 99667605 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.763 | 0.160 | 2 | 226229029 | intergenic variant | T/C | snv | 0.67 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.040 | 19 | 8404854 | downstream gene variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 6 | 159225301 | intron variant | T/C | snv | 0.38 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 16 | 67191598 | upstream gene variant | C/T | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 10 | 30027143 | missense variant | C/A;G | snv | 4.0E-06; 0.38 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 11 | 16880721 | intron variant | C/A;T | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.120 | 10 | 102836092 | intron variant | G/A;C;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.807 | 0.120 | 15 | 78796769 | missense variant | A/G | snv | 0.34 | 0.33 |
|
0.800 | 1.000 | 1 | 2011 | 2011 |